Glide 91000-GL-ARecalls & reported problems
Infinite Biomedical Technologies, LLC · For Motion Control Standard Wrist or Ottobock 10S17 Wrist Configuration · Class 2
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00850004850619), received between Mar 7, 2025 and Mar 7, 2025 — classified as 1 malfunction.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- No Apparent Adverse Event1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionMar 7, 2025No Apparent Adverse Event; No Apparent Adverse Event
IT WAS REPORTED BY THE PROSTHETIST THAT THE PATIENT WAS FEELING UNCOMFORTABLY WARM ON THE DISTAL END OF THE PROSTHESIS. PROSTHETIST ASKED THE PATIENT TO REMOVE THE PROSTHESIS IMMEDIATELY AS A PRECAUTION. THE PROSTHETISTS ALSO CHECKED THE PROSTHESIS IF THEY FELT UNCOMFORTABLY WARM, BUT THEY DID NOT FEEL THE ISSUE THE PATIENT MENTIONED. THERE WAS NO PATIENT INJURY INVOLVED IN THE CASE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21549641 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.